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FDA 510(k), K894756, DENVER PERITONEO-VENUS SHUNT
FDA 510(k), K894756, DENVER PERITONEO-VENUS SHUNT
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510(K) Number: K894756
Device Name: DENVER PERITONEO-VENUS SHUNT
Manufacturer: DONALD A LINCOLN
Device Classification Name: Shunt, Peritoneal
Regulation Number: KPM
Classification Product Code: 07/27/1989
Date Received: 09/29/1989
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: DENVER PERITONEO-VENUS SHUNT
Manufacturer: DONALD A LINCOLN
Device Classification Name: Shunt, Peritoneal
Regulation Number: KPM
Classification Product Code: 07/27/1989
Date Received: 09/29/1989
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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